supt20h Phenotypes

Phenotypes

XB-GENEPAGE-993440

Gene Symbol: supt20h Gene Name: SPT20 homolog, SAGA complex component

Expression Phenotypes Gene expression phenotype annotations where the gene of interest has been disrupted (manipulated) or is the gene assayed (assayed). Computed annotations are derived from differential expression analysis from Xenbase processed GEO data with the criteria of a TPM >= 1, FDR <= 0.05 and an absolute LogFC >= 2.
Computed annotations: supt20h assayed (3 sources)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Mouse (20 sources): abnormal allantois morphology, abnormal developmental patterning, abnormal gastrulation movements, abnormal head fold morphology, abnormal left-right axis symmetry of the somites, abnormal mesoderm development, abnormal paraxial mesoderm morphology, abnormal primitive streak morphology, abnormal retina pigment epithelium morphology, abnormal somite development, abnormal visceral yolk sac morphology, abnormal vitelline vasculature morphology, caudal body truncation, embryo tissue necrosis, embryonic growth retardation, failure of chorioallantoic fusion, failure of initiation of embryo turning, incomplete somite formation, open neural tube, prenatal lethality, incomplete penetrance [+]

Monarch Ortholog Phenotypes

These phenotypes are associated with this gene with a has phenotype relation via Monarch.

Mouse (20 sources): abnormal allantois morphology, abnormal developmental patterning, abnormal gastrulation movements, abnormal head fold morphology, abnormal left-right axis symmetry of the somites, abnormal mesoderm development, abnormal paraxial mesoderm morphology, abnormal primitive streak morphology, abnormal retina pigment epithelium morphology, abnormal somite development, [+]